| Literature DB >> 15565346 |
Hakan Mutlu1, Bilhan Paker, Nilufer Gunes, Ali Emektar, Merter Keceli, Mecit Kantarci.
Abstract
We report a case of pituitary duplication in a neonate girl whose magnetic resonance (MR) images showed unusual findings of hypogenesis of the corpus callosum and oral dermoid. Pituitary duplication is an extremely rare malformation, with only a few previously reported cases. It occurs most commonly in association with complicated midline and skull base anomalies. We present a case of this malformation with special emphasis on the hypogenesis of splenium of the corpus callosum and oral dermoid.Entities:
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Year: 2004 PMID: 15565346 DOI: 10.1007/s00234-004-1296-x
Source DB: PubMed Journal: Neuroradiology ISSN: 0028-3940 Impact factor: 2.804